Variant report

Variant	rs59234135
Chromosome Location	chr7:152853981-152853982
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:152853415..152855713-chr7:153110034..153111649,2	K562	blood:

Variant related genes	Relation type
ENSG00000234722	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10230744	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10237216	0.86[ASN][1000 genomes]
rs10240735	0.86[ASN][1000 genomes]
rs10241760	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10245112	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10251999	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10252792	0.92[ASN][1000 genomes]
rs10252850	0.91[ASN][1000 genomes]
rs10252984	0.92[ASN][1000 genomes]
rs10267609	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10267739	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10275739	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10277262	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10279034	0.92[ASN][1000 genomes]
rs10281241	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10281242	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10281358	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10808000	0.86[ASN][1000 genomes]
rs11972673	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12333398	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12333400	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1534095	0.89[ASN][1000 genomes]
rs2006236	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2311852	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2871888	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28761235	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28792774	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28812189	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28839896	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28848253	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28858768	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28892941	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4286860	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4286861	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4346923	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4346924	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4391337	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4397307	0.86[ASN][1000 genomes]
rs4413691	0.89[ASN][1000 genomes]
rs4415233	0.89[ASN][1000 genomes]
rs4463337	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4530950	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4565376	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4626511	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4726262	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6464313	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6959512	0.86[ASN][1000 genomes]
rs7778408	0.86[ASN][1000 genomes]
rs7809778	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027100	chr7:152294734-152935140	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv532221	chr7:152371297-152884547	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	nsv868873	chr7:152371297-152900113	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
4	nsv532222	chr7:152504090-153450290	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv1034937	chr7:152566162-152854895	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv831194	chr7:152762400-152963937	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv3384970	chr7:152789043-152858746	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv8233	chr7:152850690-152854803	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:152850400-152854600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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